Cathodically depositable electrodeposition paint binders based on epoxy resin-amino adducts reacted with phenol and formaldehyde modified with an unsaturated, substantially water-insoluble component

Claim 2

Process for producing cathodically depositable electrodeposition paint binders based on modified epoxy resins characterized in that- (A) 95 to 50% by weight of a reaction product obtained through reaction of an epoxy resin with at least two epoxy groups and having an epoxy equivalent weight of from about 180 to 1000 at from about 50° to 120° C. with 0.6 to 1.0 moles of primary amino groups on a primary monoalkyl amine or a primary alkylene diamine or a primary-tertiary alkylene diamine per each available epoxy group and 0 to 0.4 moles of a carboxylic compound or a secondary amine per each available epoxy group to provide an epoxy resin-amino adduct having an epoxy value of substantially zero, said epoxy resin-amino adduct thereafter being reacted at from about 50° to 90° C., calculated on one mole of NH-groups, with 0.5 to 1.0 moles phenol, and with

Claim 3

25 to 0.9 moles of formaldehyde per formaldehyde-reactive site, until the formaldehyde is substantially bound and the reaction product, upon partial or total neutralization with acids, is dilutable with water, is mixed with (B) 5 to 50% by weight of an addition component which is substantially water-insoluble under the conditions of electrodeposition and compatible with the base resin Component A, said addition component being selected from the group consisting of (a) drying oils with an iodine number of above 120; (b) synthetic esters of the fatty acids with polyols; (c) addition products of maleic anhydride to hydroxyfree drying oils with an iodine number above 120; synthetic esters of fatty acids with polyols; unsaturated hydrocarbon oligomers or polymers or copolymers with a molecular weight of from about 400 to 3000, the carboxy or anhydride groups of said maleic anhydride having been substantially completely transformed to ester, amide, or imide groups; and (d) compounds carrying at least two (meth)acrylic or allyl double bonds, the mixture, after being transformed to the water-dilutable salt by partial neutralization of the basic groups with inorganic or organic acids being dilutable with water.

Claim 4

25 to 0.9 moles of formaldehyde per formaldehyde-reactive site, until the formaldehyde is substantially bound and the reaction product, upon partial or total neutralization with acids, is dilutable with water, is mixed with (B) 5 to 50% by weight of an addition component which is substantially water-insoluble under the conditions of electrodeposition and compatible with the base resin Component A, said addition component being selected from the group consisting of (a) drying oils with an iodine number of above 120; (b) synthetic esters of the fatty acids with polyols; (c) addition products of maleic anhydride to hydroxyfree drying oils with an iodine number above 120; synthetic esters of fatty acids with polyols; unsaturated hydrocarbon oligomers or polymers or copolymers with a molecular weight of from about 400 to 3000, the carboxy or anhydride groups of said maleic anhydride having been substantially completely transformed to ester, amide, or imide groups; and (d) compounds carrying at least two (meth)acrylic or allyl double bonds, the mixture, after being transformed to the water-dilutable salt by partial neutralization of the basic groups with inorganic or organic acids being dilutable with water.

Claim 5

The process according to claim 1 wherein in Component A the epoxy resin is based on bisphenol A or a phenol novolak.

Claim 6

The process according to claim 1 wherein in Component A the amine is a primary monoalkylamine with at least four carbon atoms.

Claim 7

The process according to claim 1 wherein in Component A the amine is a blend of monoalkylamine and a alkylene diamine.

Claim 8

The process according to claim 1 wherein in Component A the reaction of the epoxy groups with the amines is carried out at 50° to 90° C.

Claim 9

The process according to claim 1 wherein in Component A the reaction of the epoxy groups with the carboxylic compounds is carried out at from 90° to 120° C.

Claim 10

The process according to claim 6 wherein in Component A the carboxylic compound is a monocarboxylic acid with 7 to 20 carbon atoms.

Claim 11

The process according to claim 6 wherein in Component A the carboxylic compound is a semiester of a dicarboxylic acid with a monoalcohol or an oxazolidine compound.

Claim 12

The process according to claim 6 wherein in Component A the carboxylic compound is an addition product of maleic acid anhydride to unsaturated oils or hydroxy-free esters of fatty acids with polyols or low molecular weight unsaturated hydrocarbon polymers or oligomers, the anhydride groups of the maleic acid anhydride having been opened through semiester formation with monohydroxy compounds.

Claim 13

The process according to claim 9 wherein in Component A the carboxylic compounds have an acid value of from 30 to 130 mg KOH/g.

Claim 14

The process according to claim 9 wherein in Component A the number of carboxy groups of the semiesters is reduced through reaction with monoepoxy compounds.

Claim 15

The process according to claim 1 wherein in Component A the said phenol is a mono- or polynuclear phenol.

Claim 16

The process according to claim 12 wherein in Component A said mono- or polynuclear phenol is substituted with an alkyl group.

Claim 17

The process according to claim 1 wherein in Component A said phenol is an amino-alkylation product of a monosubstituted or dinuclear phenol.

Claim 18

The process according to claim 1 wherein in Component A a portion of said phenol is substituted with a formaldehyde-reactive compound.

Claim 19

The process according to claim 15 wherein in Component A said formaldehyde-reactive compound is urea, melamine, or guanamine.

Claim 20

The process according to claim 1 wherein in Component A 0.1 to 0.4 moles of the phenolic compound are replaced by formaldehyde-reactive compounds selected from the group of urea, thiourea, imidourea, melamine, acetoguanamine, benzoguanamine, and mixtures thereof.

Claim 21

The process according to claim 1 wherein an auxiliary organic solvent is utilized and, after neutralization with acids and dilution with water, said solvent is at least partly vacuum-stripped from the binder combination at from 30° to 60° C.

Claim 22

The process according to claim 1 wherein the binders are pigmented and pigmentation is effected with the aid of a pigmented mill base resin.

Claim 23

Cathodically depositable electrodeposition paint binders based on modified epoxy resins comprising a mixture of (A) 95 to 50% by weight of the reaction product at from about 50° to 120° C. an epoxy resin with at least two epoxy groups and having an epoxy equivalent weight of from about 180 to 1000 with

Claim 24

Cathodically depositable electrodeposition paint binders based on modified epoxy resins comprising a mixture of (A) 95 to 50% by weight of the reaction product at from about 50° to 120° C. an epoxy resin with at least two epoxy groups and having an epoxy equivalent weight of from about 180 to 1000 with

Claim 25

6 to 1.0 moles of primary amino groups on a primary monoalkyl amine or a primary alkylene diamine or a primary-tertiary alkylene diamine per each available epoxy group and 0 to 0.4 moles of a carboxylic compound or a secondary amine per each available epoxy group to provide an epoxy resin-amino adduct having an epoxy value of substantially zero, said epoxy resin-amino adduct thereafter being reacted at from about 50° to 90° C. per mole of NH-groups, with 0.5 to 1.0 moles phenol and 0.25 to 0.9 moles of formaldehyde per formaldehyde-reactive site to provide a product wherein said formaldehyde is substantially bound and said reaction product, upon partial or total neutralization with acids, is dilutable with water, and (B) 5 to 50% by weight of an addition component which is substantially water-insoluble under the conditions of electrodeposition and compatible with the base resin Component A, said addition component being selected from the group consisting of (a) drying oils with an iodine number of above 120; (b) synthetic esters of the fatty acids with polyols; (c) addition products of maleic anhydride to hydroxy-free drying oils with an iodine number above 120; synthetic esters of fatty acids with polyols; unsaturated hydrocarbon oligomers or polymers or copolymers with a molecular weight of from about 400 to 3000, the carboxy or anhydride groups of said maleic anhydride having been substantially completely transformed to ester, amide, or imide groups; and (d) compounds carrying at least two (meth)acrylic or allyl double bonds, the mixture, after being transformed to the water-dilutable salt by partial neutralization of the basic groups with inorganic or organic acids being dilutable with water.

Claim 26

6 to 1.0 moles of primary amino groups on a primary monoalkyl amine or a primary alkylene diamine or a primary-tertiary alkylene diamine per each available epoxy group and 0 to 0.4 moles of a carboxylic compound or a secondary amine per each available epoxy group to provide an epoxy resin-amino adduct having an epoxy value of substantially zero, said epoxy resin-amino adduct thereafter being reacted at from about 50° to 90° C. per mole of NH-groups, with 0.5 to 1.0 moles phenol and 0.25 to 0.9 moles of formaldehyde per formaldehyde-reactive site to provide a product wherein said formaldehyde is substantially bound and said reaction product, upon partial or total neutralization with acids, is dilutable with water, and (B) 5 to 50% by weight of an addition component which is substantially water-insoluble under the conditions of electrodeposition and compatible with the base resin Component A, said addition component being selected from the group consisting of (a) drying oils with an iodine number of above 120; (b) synthetic esters of the fatty acids with polyols; (c) addition products of maleic anhydride to hydroxy-free drying oils with an iodine number above 120; synthetic esters of fatty acids with polyols; unsaturated hydrocarbon oligomers or polymers or copolymers with a molecular weight of from about 400 to 3000, the carboxy or anhydride groups of said maleic anhydride having been substantially completely transformed to ester, amide, or imide groups; and (d) compounds carrying at least two (meth)acrylic or allyl double bonds, the mixture, after being transformed to the water-dilutable salt by partial neutralization of the basic groups with inorganic or organic acids being dilutable with water.

Claim 27

The binder according to claim 20 wherein in Component A the said phenol is a mono- or polynuclear phenol.

Claim 28

The binder according to claim 20 wherein in Component A said mono- or polynuclear phenol is substituted with an alkyl group.

Claim 29

The binder according to claim 20 wherein in Component A said phenol is an amino-alkylation product of a monosubstituted or dinuclear phenol.

Claim 30

The binder according to claim 20 wherein in Component A a portion of said phenol is substituted with a formaldehyde-reactive compound.

Claim 31

The binder according to claim 20 wherein in Component A the epoxy resin is based on bisphenol A or a phenol novolak.

Claim 32

The binder according to claim 20 wherein in Component A the amine is a primary monoalkylamine with at least four carbon atoms.

Claim 33

The binder according to claim 20 wherein in Component A the amine is a blend of primary monoalkylamines and primary alkylene diamines.

Claim 34

The binder according to claim 20 wherein in Component A the carboxylic compound is a monocarboxylic acid which has from 7 to 20 carbon atoms.

Claim 35

The binder according to claim 28 wherein in Component A the carboxylic compound is an addition product of maleic acid anhydride to an unsaturated oil or the hydroxy-free esters of an oil fatty acid with a polyol or a low molecular weight unsaturated hydrocarbon polymer or oligomer, the anhyride groups of maleic acid having been opened through semiester formation with a monohydroxy compound.